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Science Review Board
Results: 2734

#	Item
151	Research Ethics Checklist (SHUREC1) This form is designed to help staff and students to complete an ethical scrutiny of proposed research. The SHU Research Ethics Policy should be consulted before completing the form. An Add to Reading List Source URL: www.shu.ac.uk Language: English - Date: 2014-10-09 09:27:04 Science Clinical research Design of experiments Pharmacology Data collection Research ethics Institutional review board Question Informed consent Applied ethics Medical ethics Ethics
152	Office of Human Research Ethics Daniel Nelson, Director T Add to Reading List Source URL: research.unc.edu Language: English - Date: 2012-11-27 10:01:04 Science Institutional review board Public Responsibility in Medicine and Research National Institutes of Health Adverse event North Carolina Research Campus Human subject research Grant Certified IRB Professional Clinical research Research Medicine
153	Consent process for medical research conflicts with standard UK practice Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2015-05-27 20:06:09 Ethics Clinical research Biological databases Research ethics Pharmacology Institutional review board Biobank Informed consent Biobank ethics Applied ethics Medical ethics Science
154	3.2 ADVERSE EVENT (AE) PROCESS & FORMS Serious Adverse Events (SAEs), Suspected Unexpected Serious Adverse Reactions (SUSARs), annual trial safety updates and other related safety information are Add to Reading List Source URL: www.sjog.org.au Language: English - Date: 2014-10-30 00:26:29 Pharmacology Science Health Design of experiments Patient safety Clinical trial Adverse effect Institutional review board Serious adverse event Clinical research Research Pharmaceutical industry
155	CLINICAL TRIALS What are they? How are they designed and conducted? What safeguards are there? Add to Reading List Source URL: www.slhd.nsw.gov.au Language: English - Date: 2005-12-01 17:50:47 Health Design of experiments Pharmaceutical industry Pharmacology Medical statistics Clinical trial Medical research Medical ethics Institutional review board Research Clinical research Science
156	Saint Leo University Institutional Review Board – Application for IRB Review of Proposed Research All Word processor files should be combined into ONE file for submission, with supplemental files placed Add to Reading List Source URL: www.saintleo.edu Language: English - Date: 2015-01-23 08:44:05 Research Design of experiments Pharmacology Behavior Drug safety Institutional review board Informed consent Email Psychology Clinical research Medical ethics Science
157	Guido Rasi, Executive Director, AIFA In welcoming all the participants to the Round Table today, I would like to underline the reasons that induced the Italian Medicines Agency to support this initiative and the general Add to Reading List Source URL: www.unicri.it Language: English - Date: 2009-04-28 09:23:48 Science Pharmacology Pharmaceutical sciences Design of experiments Clinical trials Good Clinical Practice Institutional review board Declaration of Helsinki European Forum for Good Clinical Practice Clinical research Research Pharmaceutical industry
158	GENERAL ASPECTS AND PRINCIPLES OF ICHGCP (GOOD CLINICAL PRACTICE) Umberto Filibeck Former Head of AIFA GCP Inspectorate and GCP Promotion Unit UNICRI Consultant for Projects on GCP of CTs in developing countries Add to Reading List Source URL: www.unicri.it Language: English - Date: 2012-08-07 10:48:19 Scientific method Institutional review board Good Clinical Practice Clinical trial Clinical site Declaration of Helsinki Ethics Committee Regulatory requirement Protocol Clinical research Research Science
159	INSPECTION OF INDEPENDENT ETHICS COMMITTEES (IEC) The Italian Experience Umberto Filibeck Former Head of AIFA GCP Inspectorate and GCP Promotion Unit UNICRI Consultant for Projects on GCP of CTs in developing countries Add to Reading List Source URL: www.unicri.it Language: English - Date: 2012-08-07 10:48:19 Scientific method Institutional review board Clinical trial Clinical Trials Directive Declaration of Helsinki Ethics Committee Informed consent Clinical site Clinical research coordinator Clinical research Research Science
160	Conservatoires UK (CUK) Ethical Approval Form for staff and student questionnaire research with adults only Type of project: STAFF / POSTGRADUATE / UNDERGRADUATE (delete as appropriate) Title of project: Add to Reading List Source URL: www.conservatoiresuk.ac.uk Language: English - Date: 2015-03-16 05:12:54 Scientific method Evaluation methods Medical ethics Marketing Market research Survey methodology Questionnaire Informed consent Institutional review board Science Research methods Statistics

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